A qualitative study of patient and professional perspectives of healthcare services for multiple sclerosis

implications for service development and policy

Abigail M. Methley, Carolyn A. Chew-Graham, Sudeh Cheraghi-Sohi, Stephen M. Campbell

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

Multiple sclerosis (MS) is a chronic degenerative condition, with heterogeneous symptoms, and an unpredictable prognosis. Previous literature suggests patients' experiences of healthcare are unsatisfactory. Primary care may play a key role in the management of people with MS (PwMS); however, provision of services for PwMS has received little focus in the primary care literature. This study aimed to explore perspectives and experiences of PwMS and healthcare professionals of UK healthcare services for MS. Semi-structured interviews were conducted with 24 PwMS, 13 Practice Nurses, 12 General Practitioners and 9 MS Specialist Nurses in northern England, between October 2012 and April 2014. Participants were purposively selected. Data were analysed thematically using constant comparative analysis. The theoretical framework of candidacy was used to interrogate data, with themes mapping onto the National Institute for Health and Care Excellence (NICE) guideline for MS. How PwMS interpreted symptoms as leading to candidacy for care dictated help-seeking. PwMS required additional support in identifying symptoms due to MS. Participants reported poor experiences of care including poor access to services, poor continuity of care and poor interpersonal interactions with perceptions of limited person-centredness. PwMS and professionals identified that MS-related disability and progression of symptoms required responsive care. Relational continuity enabled PwMS to feel understood, and professionals to holistically appraise symptoms and progression. In conclusion, continuity and patient-centredness of care are central to positive healthcare experiences for PwMS and professionals. Services need to be more accessible to ensure responsive and effective MS management. This study provides unique findings on the role of primary care for PwMS, and the relationship between findings and MS NICE guideline recommendations with implications for service delivery in the community.

Original languageEnglish
Pages (from-to)848-857
Number of pages10
JournalHealth and Social Care in the Community
Volume25
Issue number3
DOIs
Publication statusPublished - May 2017
Externally publishedYes

Fingerprint

multiple sclerosis
Policy Making
Multiple Sclerosis
Delivery of Health Care
Primary Health Care
Continuity of Patient Care
continuity
National Institutes of Health (U.S.)
experience
nurse
Guidelines
candidacy
England
general practitioner
General Practitioners
health
management
Nurses
Interviews
disability

Cite this

Methley, Abigail M. ; Chew-Graham, Carolyn A. ; Cheraghi-Sohi, Sudeh ; Campbell, Stephen M. / A qualitative study of patient and professional perspectives of healthcare services for multiple sclerosis : implications for service development and policy. In: Health and Social Care in the Community. 2017 ; Vol. 25, No. 3. pp. 848-857.
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abstract = "Multiple sclerosis (MS) is a chronic degenerative condition, with heterogeneous symptoms, and an unpredictable prognosis. Previous literature suggests patients' experiences of healthcare are unsatisfactory. Primary care may play a key role in the management of people with MS (PwMS); however, provision of services for PwMS has received little focus in the primary care literature. This study aimed to explore perspectives and experiences of PwMS and healthcare professionals of UK healthcare services for MS. Semi-structured interviews were conducted with 24 PwMS, 13 Practice Nurses, 12 General Practitioners and 9 MS Specialist Nurses in northern England, between October 2012 and April 2014. Participants were purposively selected. Data were analysed thematically using constant comparative analysis. The theoretical framework of candidacy was used to interrogate data, with themes mapping onto the National Institute for Health and Care Excellence (NICE) guideline for MS. How PwMS interpreted symptoms as leading to candidacy for care dictated help-seeking. PwMS required additional support in identifying symptoms due to MS. Participants reported poor experiences of care including poor access to services, poor continuity of care and poor interpersonal interactions with perceptions of limited person-centredness. PwMS and professionals identified that MS-related disability and progression of symptoms required responsive care. Relational continuity enabled PwMS to feel understood, and professionals to holistically appraise symptoms and progression. In conclusion, continuity and patient-centredness of care are central to positive healthcare experiences for PwMS and professionals. Services need to be more accessible to ensure responsive and effective MS management. This study provides unique findings on the role of primary care for PwMS, and the relationship between findings and MS NICE guideline recommendations with implications for service delivery in the community.",
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A qualitative study of patient and professional perspectives of healthcare services for multiple sclerosis : implications for service development and policy. / Methley, Abigail M.; Chew-Graham, Carolyn A.; Cheraghi-Sohi, Sudeh; Campbell, Stephen M.

In: Health and Social Care in the Community, Vol. 25, No. 3, 05.2017, p. 848-857.

Research output: Contribution to journalArticle

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